Specific probiotics and prebiotics to improve the quality of life of patients with chronic irritable bowel syndrome.

IF 1.9 Q3 GASTROENTEROLOGY & HEPATOLOGY Minerva gastroenterology Pub Date : 2024-01-19 DOI:10.23736/S2724-5985.23.03563-5
Lorenzo Bertani, Linda Balestrini, Lucia Chico, Giulia Della Scala, Francesca Geri, Alessandro Tornar, Claudio Belcari
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Abstract

Background: Irritable bowel syndrome (IBS) is a chronic disorder with an important impact on patients' quality of life. Although several data indicate that psychological symptoms are frequently reported by patients with IBS, few therapies have been evaluated regarding these issues.

Methods: A retrospective observational study was conducted to evaluate the effectiveness of a probiotic-based dietary supplement (Colicron®) in a group of patients with diarrhea-predominant IBS (IBS-D). We included patients treated with Colicron® (1 cps/day for 8 weeks). Primary endpoint was the gastrointestinal symptoms' remission evaluated by Visual Analogue Scale (VAS); secondary endpoint was the impact of the treatment on physical and mental health evaluated by Hospital Anxiety and Depression Score (HADS) and Short Form Health Survey 36 (SF-36). VAS was assessed at week 4 (T4), week 8 (T8) and week 12 (T12), whereas HADS and SF-36 were performed even at the start of the Colicron® treatment (T0).

Results: An improvement of VAS Score was observed at T8 (P<0.001) and T12 (P<0.05) compared to T4. Lower HADS-A (anxiety subdomain) score was obtained at each time point versus T0 (P<0.01), and higher scores of all SF-36 domains were observed during the treatment (0.05

Conclusions: Colicron® could be useful in improving both gastrointestinal and psychological symptoms in IBS-D patients. Further prospective clinical trials are needed to confirm these preliminary data.

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改善慢性肠易激综合征患者生活质量的特定益生菌和益生元。
背景:肠易激综合征(IBS肠易激综合征(IBS)是一种慢性疾病,对患者的生活质量有重要影响。虽然有一些数据表明肠易激综合征患者经常会出现心理症状,但很少有治疗方法对这些问题进行评估:我们开展了一项回顾性观察研究,以评估一种基于益生菌的膳食补充剂(Colicron®)对一组腹泻为主的肠易激综合征(IBS-D)患者的疗效。研究对象包括接受 Colicron®(1 cps/天,为期 8 周)治疗的患者。主要研究终点是通过视觉模拟量表(VAS)评估胃肠道症状的缓解情况;次要研究终点是通过医院焦虑抑郁评分(HADS)和 36 项简表健康调查(SF-36)评估治疗对身心健康的影响。VAS在第4周(T4)、第8周(T8)和第12周(T12)进行评估,而HADS和SF-36则在可立康®治疗开始时(T0)进行评估:结果:在治疗第 8 周(PC)时,VAS 评分有所改善:结论:可立克龙®可有效改善肠易激综合征(IBS-D)患者的胃肠道症状和心理症状。需要进一步的前瞻性临床试验来证实这些初步数据。
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